Chair conformational isomer

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chiddler

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I'm looking at basic cyclohexane. Is it accurate to describe the most stable conformational isomers of carbon out of plane-carbon in plane as gauche? What about the other carbons?

Meaning what conformational isomer form (anti, gauche) are carbons-carbon bonds in a cyclohexane in?

I didn't really think of bonds in a chair as having conformational isomers, but TBR is cool like that.
 
I'm looking at basic cyclohexane. Is it accurate to describe the most stable conformational isomers of carbon out of plane-carbon in plane as gauche? What about the other carbons?

Meaning what conformational isomer form (anti, gauche) are carbons-carbon bonds in a cyclohexane in?

I didn't really think of bonds in a chair as having conformational isomers, but TBR is cool like that.

I didn't know you could think of the carbons in cyclohexane as gauche or anti. I thought those terms were for substituents on the cyclohexane.
 
I didn't know you could think of the carbons in cyclohexane as gauche or anti. I thought those terms were for substituents on the cyclohexane.

Makes sense...

XoRIJ.png


What should I make of this question? Not asking for an explanation of the question per se (I understand it), but rather: what are the implications of a question like this?
 
Makes sense...

XoRIJ.png


What should I make of this question? Not asking for an explanation of the question per se (I understand it), but rather: what are the implications of a question like this?


Just knowing that interactions only occur between substituents on neighboring carbons. So 1,4 substituents don't interact with each other.

I know you said you aren't asking an explanation, but this will help me and maybe ring a bell in your head as well. For answer A, gauche CH3/H means the CH3 on Carbon 1 with an H on Carbon 2 and/or Carbon 6. Or it could mean the CH3 on Carbon 4 with an H on Carbon 3 and/or Carbon 5. Same is true for B, except anti instead of gauche.
 
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